US4270923A - Pretreatment agent for subject fluid in pregnancy test - Google Patents
Pretreatment agent for subject fluid in pregnancy test Download PDFInfo
- Publication number
- US4270923A US4270923A US06/107,179 US10717979A US4270923A US 4270923 A US4270923 A US 4270923A US 10717979 A US10717979 A US 10717979A US 4270923 A US4270923 A US 4270923A
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- United States
- Prior art keywords
- fiber
- glass fiber
- cation exchange
- subject fluid
- carboxylic acid
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- 239000012530 fluid Substances 0.000 title claims abstract description 30
- 238000009597 pregnancy test Methods 0.000 title claims abstract description 7
- 239000000835 fiber Substances 0.000 claims abstract description 50
- 239000003365 glass fiber Substances 0.000 claims abstract description 40
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 239000003729 cation exchange resin Substances 0.000 claims abstract description 28
- 230000001900 immune effect Effects 0.000 claims abstract description 7
- 230000002452 interceptive effect Effects 0.000 claims abstract description 6
- 108010062540 Chorionic Gonadotropin Proteins 0.000 claims abstract description 3
- 102000011022 Chorionic Gonadotropin Human genes 0.000 claims abstract description 3
- 229940084986 human chorionic gonadotropin Drugs 0.000 claims abstract description 3
- 210000002700 urine Anatomy 0.000 claims description 35
- 238000000034 method Methods 0.000 claims description 15
- 210000002966 serum Anatomy 0.000 claims description 15
- 238000005341 cation exchange Methods 0.000 claims description 3
- 238000003556 assay Methods 0.000 claims description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 2
- 229920005989 resin Polymers 0.000 claims description 2
- 239000011347 resin Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 description 19
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 17
- 229920000742 Cotton Polymers 0.000 description 17
- 238000001914 filtration Methods 0.000 description 17
- 229920002239 polyacrylonitrile Polymers 0.000 description 17
- 229920002301 cellulose acetate Polymers 0.000 description 16
- 239000001768 carboxy methyl cellulose Substances 0.000 description 15
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 15
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 15
- 229940105329 carboxymethylcellulose Drugs 0.000 description 15
- -1 polyethylene Polymers 0.000 description 13
- 239000004816 latex Substances 0.000 description 12
- 229920000126 latex Polymers 0.000 description 12
- 239000004677 Nylon Substances 0.000 description 9
- 229920000297 Rayon Polymers 0.000 description 9
- 229920001778 nylon Polymers 0.000 description 9
- 229920000728 polyester Polymers 0.000 description 9
- 229920002635 polyurethane Polymers 0.000 description 9
- 239000004814 polyurethane Substances 0.000 description 9
- 229920000915 polyvinyl chloride Polymers 0.000 description 9
- 239000004800 polyvinyl chloride Substances 0.000 description 9
- 230000035935 pregnancy Effects 0.000 description 9
- 239000004743 Polypropylene Substances 0.000 description 8
- 230000004520 agglutination Effects 0.000 description 8
- 229920001155 polypropylene Polymers 0.000 description 8
- 210000002268 wool Anatomy 0.000 description 8
- 238000003745 diagnosis Methods 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 230000005764 inhibitory process Effects 0.000 description 6
- 238000002203 pretreatment Methods 0.000 description 6
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- 210000004209 hair Anatomy 0.000 description 4
- 231100000640 hair analysis Toxicity 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 238000001179 sorption measurement Methods 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 210000002381 plasma Anatomy 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 210000003743 erythrocyte Anatomy 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010029719 Nonspecific reaction Diseases 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000003759 clinical diagnosis Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000002405 diagnostic procedure Methods 0.000 description 1
- 230000035931 haemagglutination Effects 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000012092 latex agglutination test Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000003127 radioimmunoassay Methods 0.000 description 1
- 230000036647 reaction Effects 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/74—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors
- G01N33/76—Human chorionic gonadotropin including luteinising hormone, follicle stimulating hormone, thyroid stimulating hormone or their receptors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/811—Test for named disease, body condition or organ function
- Y10S436/814—Pregnancy
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/815—Test for named compound or class of compounds
- Y10S436/817—Steroids or hormones
- Y10S436/818—Human chorionic gonadotropin
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/825—Pretreatment for removal of interfering factors from sample
Definitions
- the present invention relates to an improvement in the pretreatment of subject fluids for immunologic pregnancy tests.
- HCG human chorionic gonadotropin
- the principle of the anti-HCG antibody-sensitized latex agglutination test is that as a latex particles carrying anti-HCG antibodies as adsorbed thereon are admixed with a subject urine, serum or plasma sample, the latex particles are agglutinated if HCG is present in the sample, the detection of such agglutination establishing a diagnosis of pregnancy.
- LDAR latex direct agglutination reaction
- the principle of the HCG-sensitized latex agglutination inhibition test (latex agglutination inhibition reaction; hereinafter briefly, LAIR), is that as a latex carrying HCG as adsorbed thereon is admixed with a given amount of an anti-HCG antiserum, the latex particles are agglutinated, but if the latex is added after admixture of an HCG-containing subject fluid with a given amount of anti-HCG antiserum, the latex will not be agglutinated because the anti-HCG antibody has already been coupled to the HCG in the subject fluid.
- LAIR the absence of latex agglutination establishes a diagnosis of pregnancy.
- Another method is the hemagglutination inhibition test (hereinafter briefly, HAIR) in which a diagnosis of pregnancy is performed using HCG-sensitized human or animal red blood cells in place of latex particles.
- Subject fluids could also be turbid and if such fluids are directly assayed, false results may ensue. To prevent such false results, the fluids are usually filtered prior to the agglutination (inhibition) reaction.
- the filter materials conventionally employed are cellulosic filter paper, absorbent cotton, cellulose acetate, polyacrylonitrile, carboxylmethylcellulose and other fiber but none of them is fully satisfactory.
- cellulosic filter paper and absorbent cotton are capable of removing the turbidity but have the disadvantage that HCG is also adsorbed.
- Cellulose acetate and polyacrylonitrile fiber are not efficient enough to thoroughly remove interferring components.
- fibrous carboxylmethylcellulose is highly capable of removing the turbidity and interfering components, it entails adsorption of HCG.
- the present inventors have unexpectedly found that the interfering components and the elements of turbidity present in the subject fluids can be specifically removed without entailing a substantial loss of HCG by contacting the subject fluids with a carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber.
- the principal object of the present invention is to provide an excellent agent for pretreating a subject fluid for pregnancy tests by means of an immunologic assay of HCG, which consists essentially of a carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber. Another object is to provide an improved method for pretreating the subject fluids with use of said agent.
- the carboxylic acid-type cation exchange resin fiber used in this invention preferably has a cation exchange capacity of at least about 1.5 meq/g and, especially, about 5 to 8 meq/g.
- a preferable fiber may be prepared by reacting a polymer molding containing at least 40 weight percent of acrylonitrile with hydrazine or a homolog of hydrazine to provide said polymer molding with an anion exchange capacity of 0.01 to 3.0 meq/g and, then, hydrolyzing the residual nitrile groups with alkali or mineral acid to introduce cation-exchanging groups into the molding (cf. Japanese Patent Application Laid-Open No. 14389/1974 (Tokukai Sho 49-14389)).
- the siliconized glass fiber may be prepared by treating an ordinary glass fiber with a compound of silicon or a silicon-containing composition such as silane coupling agents (organofunctional silanes), silicone oil, silicone oil emulsion, silicone varnish, silicone varnish emulsion, etc.
- a compound of silicon or a silicon-containing composition such as silane coupling agents (organofunctional silanes), silicone oil, silicone oil emulsion, silicone varnish, silicone varnish emulsion, etc.
- This siliconization treatment is generally carried out by impregnating a glass fiber with an aqueous or organic solvent solution of said compound of silicon or silicon-containing composition and heating the fiber (usually at about 100° to 300° C.).
- the carboxylic acid-type cation exchange resin fiber and siliconized glass fiber may be used alone or in combination.
- the carboxylic acid-type cation exchange resin fiber is advantageously used in the form of filament or staple fiber (preferably 0.1 to 2 mm in length) with a denier number of about 2 to 15.
- the siliconized glass fiber is preferably used in the form of filament with a diameter of about 5 to 15 ⁇ m.
- the fluid In contacting the subject fluid, such as the urine, serum or plasma of a woman, with the above-mentioned fiber, the fluid may be filtered through a layer of the fiber or, alternatively, the fluid may be admixed with the fiber and then separated (by filtration, centrifugal separation, etc.), although it is generally preferable to filter the subject fluid through the fibrous layer.
- a typical filtration procedure is as follows. A tube (preferably made from polyethylene) is packed with about 20 to 100 mg, most preferably about 50 mg, of said fiber and connected to the lower end of a pipe (preferably made from polyethylene) fitted with a rubber suction cap.
- the tube is dipped into the subject fluid and the rubber cap is squeezed to fill the suction pipe with a suitable quantity (about 0.3 ml) of the test fluid to obtain a filtrate.
- the tube is disconnected and the filtrate is directly used for the pregnancy diagnostic test. For instance, two drops of the above filtrate are dripped on a clean glass plate for LDAR or LAIR, or a HAIR test is carried out with 0.1 ml in a test tube.
- the present invention further provides a kit for the pretreatment of the subject fluids, which comprises a tube packed with about 20 to 100 mg of the carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber, and a pipe fitted with a rubber suction cap, to which said tube is to be connected at its lower end.
- the pretreatment according to this invention removes the interfering components and turbidity elements without causing any substantial loss of HCG in the subject fluid, thus leading to remarkable improvements in sensitivity and reliability of the pregnancy test, especially LDAR.
- carboxylic acid-type cation exchange resin fiber and siliconized glass fiber used in these tests and examples are as follows:
- the carboxylic acid-type cation exchange resin fiber was prepared by the procedure described in Example 1 of Japanese Patent Application Laid-Open No. 14389/1974. It has a triazine-or tetrazine-cross linked structure and a cation exchange capacity of 6.4 meq/g, and is a pale-pinkish in appearance. In the infrared region of the spectrum this fiber showed a strong carbonyl band at 1600-1700 cm -1 but showed no nitrile absorption (2250 cm -1 ). This resin fiber was used in the form of filament with 6 denier except Example 4 wherein it was used in the form of staple fiber of 1 mm inn length with 3 denier.
- the siliconized glass fiber was prepared as follows. A glass fiber with a diameter of about 10 ⁇ m was dewaxed with acetone and diethyl ether, immersed in a 1% solution of dimethylpolysiloxane in trichloroethylene for one minute, heat-treated at 200° C. for one hour and finally washed with 20% ethanol.
- the filters of this invention effectively remove the components which would interfere with the reactions. Thus, they reduce considerably the incidence of misdiagnosing nonpregnancy as pregnancy.
- HCG was added to 3 urine samples from healthy nonpregnant women to give an HCG concentration of one I.U./ml, and each sample was filtered as described hereinbefore. The residual HCG (%) in each filtered urine sample was measured by radioimmunoassay.
- cellulosic filter paper absorbent cotton, wool, untreated glass fiber, viscose rayon, nylon, polyester, polypropylene, polyvinyl chloride, polyurethane and carboxymethylcellulose showed up to 65% adsorption of HCG. Substantially no adsorption of HCG occurred with carboxylic acid-type cation exchange resin fiber, siliconized glass fiber, cellulose acetate or polyacrylonitrile fiber.
- Polyethylene tubes 5.0 mm in inside diameter, were respectively packed with 50 mg of carboxylic acid-type cation exchange resin fiber or siliconized glass fiber of the present invention, absorbent cotton, cellulose acetate fiber, polyacrylonitrile fiber and carboxymethylcellulose fiber and 400 urine samples from nonpregnant women were filtered with the above tubes by the procedure described hereinbefore, to obtain 0.3 ml of filtered urine from each urine sample. Two drops of each filtered urine sample were subjected to the LDAR tests.
- Urine samples from 200 women definitely diagnosed as pregnant by clinical diagnoses were subjected to the LDAR test after filtration under the same conditions as in Example 1 using the carboxylic acid-type cation exchange resin fiber or siliconized glass fiber of the present invention or absorbent cotton, cellulose acetate fiber, polyacrylonitrile fiber or carboxymethylcellulose fiber.
- Serum samples from 50 nonpregnant women and 50 pregnant women were filtered through the carboxylic acid-type cation exchange resin fiber or siliconized glass fiber used as a filter material under the same conditions as in Example 1 and two drops of each filtered serum sample were subjected to the LDAR test. All the serum samples from nonpregnant women reacted negatively, while all the serum samples from pregnant women showed positive reactions.
- Urine samples from 50 nonpregnant women and 50 pregnant women were filtered through the carboxylic acid-type cation exchange resin staple fiber of 1 mm in length with 3 denier used as a filter material under the same conditions as in Example 1 and two drops of each filtered urine samples were subjected to the LDAR test. All the urine samples from nonpregnant women reacted negatively, while all the urine sample from pregnant women showed positive reactions.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Medicinal Chemistry (AREA)
- Analytical Chemistry (AREA)
- Cell Biology (AREA)
- Biotechnology (AREA)
- Food Science & Technology (AREA)
- Reproductive Health (AREA)
- Physics & Mathematics (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Filtering Materials (AREA)
Abstract
By using a new pretreatment agent consisting essentially of a carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber, the interfering components and the elements of turbidity present in a subject fluid for immunologic pregnancy test can be specifically removed without entailing a substantial loss of human chorionic gonadotropin contained in the subject fluid.
Description
The present invention relates to an improvement in the pretreatment of subject fluids for immunologic pregnancy tests.
Immunologic tests have been used for the diagnosis of pregnancy, which estimate the human chorionic gonadotropin (hereinafter briefly, HCG) in the urine or body fluid (serum, plasma, etc.) of a pregnant woman.
The principle of the anti-HCG antibody-sensitized latex agglutination test (latex direct agglutination reaction; hereinafter briefly, LDAR) is that as a latex particles carrying anti-HCG antibodies as adsorbed thereon are admixed with a subject urine, serum or plasma sample, the latex particles are agglutinated if HCG is present in the sample, the detection of such agglutination establishing a diagnosis of pregnancy. On the other hand, the principle of the HCG-sensitized latex agglutination inhibition test (latex agglutination inhibition reaction; hereinafter briefly, LAIR), is that as a latex carrying HCG as adsorbed thereon is admixed with a given amount of an anti-HCG antiserum, the latex particles are agglutinated, but if the latex is added after admixture of an HCG-containing subject fluid with a given amount of anti-HCG antiserum, the latex will not be agglutinated because the anti-HCG antibody has already been coupled to the HCG in the subject fluid. This, in LAIR the absence of latex agglutination establishes a diagnosis of pregnancy. Another method is the hemagglutination inhibition test (hereinafter briefly, HAIR) in which a diagnosis of pregnancy is performed using HCG-sensitized human or animal red blood cells in place of latex particles.
These immunologic pregnancy tests tend to give false results in early stages of pregnancy because the secretion of HCG in this period is so small that only a weak agglutination (or inhibition) reaction takes place. Moreover, sensitized latex and sensitized red blood cells may undergo non-specific reactions independently of the immunologic reaction of HCG with the anti-HCG antibody. Therefore, when the urine or serum containing a variety of components is assayed by the above methods, the agglutination (or inhibition) reaction is interfered with by components other than HCG in the sample to lead to a false diagnosis.
Subject fluids could also be turbid and if such fluids are directly assayed, false results may ensue. To prevent such false results, the fluids are usually filtered prior to the agglutination (inhibition) reaction.
The filter materials conventionally employed are cellulosic filter paper, absorbent cotton, cellulose acetate, polyacrylonitrile, carboxylmethylcellulose and other fiber but none of them is fully satisfactory. For instance, cellulosic filter paper and absorbent cotton are capable of removing the turbidity but have the disadvantage that HCG is also adsorbed. Cellulose acetate and polyacrylonitrile fiber are not efficient enough to thoroughly remove interferring components. While fibrous carboxylmethylcellulose is highly capable of removing the turbidity and interfering components, it entails adsorption of HCG.
With the above technical difficulties by way of background, the present inventors have unexpectedly found that the interfering components and the elements of turbidity present in the subject fluids can be specifically removed without entailing a substantial loss of HCG by contacting the subject fluids with a carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber.
Thus, the principal object of the present invention is to provide an excellent agent for pretreating a subject fluid for pregnancy tests by means of an immunologic assay of HCG, which consists essentially of a carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber. Another object is to provide an improved method for pretreating the subject fluids with use of said agent. Other objects will be made clear from the description and claims hereinafter.
The carboxylic acid-type cation exchange resin fiber used in this invention preferably has a cation exchange capacity of at least about 1.5 meq/g and, especially, about 5 to 8 meq/g. For example, a preferable fiber may be prepared by reacting a polymer molding containing at least 40 weight percent of acrylonitrile with hydrazine or a homolog of hydrazine to provide said polymer molding with an anion exchange capacity of 0.01 to 3.0 meq/g and, then, hydrolyzing the residual nitrile groups with alkali or mineral acid to introduce cation-exchanging groups into the molding (cf. Japanese Patent Application Laid-Open No. 14389/1974 (Tokukai Sho 49-14389)).
The siliconized glass fiber may be prepared by treating an ordinary glass fiber with a compound of silicon or a silicon-containing composition such as silane coupling agents (organofunctional silanes), silicone oil, silicone oil emulsion, silicone varnish, silicone varnish emulsion, etc. This siliconization treatment is generally carried out by impregnating a glass fiber with an aqueous or organic solvent solution of said compound of silicon or silicon-containing composition and heating the fiber (usually at about 100° to 300° C.).
The carboxylic acid-type cation exchange resin fiber and siliconized glass fiber may be used alone or in combination. The carboxylic acid-type cation exchange resin fiber is advantageously used in the form of filament or staple fiber (preferably 0.1 to 2 mm in length) with a denier number of about 2 to 15. The siliconized glass fiber is preferably used in the form of filament with a diameter of about 5 to 15 μm.
In contacting the subject fluid, such as the urine, serum or plasma of a woman, with the above-mentioned fiber, the fluid may be filtered through a layer of the fiber or, alternatively, the fluid may be admixed with the fiber and then separated (by filtration, centrifugal separation, etc.), although it is generally preferable to filter the subject fluid through the fibrous layer. A typical filtration procedure is as follows. A tube (preferably made from polyethylene) is packed with about 20 to 100 mg, most preferably about 50 mg, of said fiber and connected to the lower end of a pipe (preferably made from polyethylene) fitted with a rubber suction cap. Then, the tube is dipped into the subject fluid and the rubber cap is squeezed to fill the suction pipe with a suitable quantity (about 0.3 ml) of the test fluid to obtain a filtrate. The tube is disconnected and the filtrate is directly used for the pregnancy diagnostic test. For instance, two drops of the above filtrate are dripped on a clean glass plate for LDAR or LAIR, or a HAIR test is carried out with 0.1 ml in a test tube.
The present invention further provides a kit for the pretreatment of the subject fluids, which comprises a tube packed with about 20 to 100 mg of the carboxylic acid-type cation exchange resin fiber or a siliconized glass fiber, and a pipe fitted with a rubber suction cap, to which said tube is to be connected at its lower end.
The pretreatment according to this invention removes the interfering components and turbidity elements without causing any substantial loss of HCG in the subject fluid, thus leading to remarkable improvements in sensitivity and reliability of the pregnancy test, especially LDAR.
The beneficial results of this invention will be further explained by the following tests and working examples.
The carboxylic acid-type cation exchange resin fiber and siliconized glass fiber used in these tests and examples are as follows:
The carboxylic acid-type cation exchange resin fiber was prepared by the procedure described in Example 1 of Japanese Patent Application Laid-Open No. 14389/1974. It has a triazine-or tetrazine-cross linked structure and a cation exchange capacity of 6.4 meq/g, and is a pale-pinkish in appearance. In the infrared region of the spectrum this fiber showed a strong carbonyl band at 1600-1700 cm-1 but showed no nitrile absorption (2250 cm-1). This resin fiber was used in the form of filament with 6 denier except Example 4 wherein it was used in the form of staple fiber of 1 mm inn length with 3 denier.
The siliconized glass fiber was prepared as follows. A glass fiber with a diameter of about 10 μm was dewaxed with acetone and diethyl ether, immersed in a 1% solution of dimethylpolysiloxane in trichloroethylene for one minute, heat-treated at 200° C. for one hour and finally washed with 20% ethanol.
In the following tests and examples, LDAR and HAIR tests were respectively performed in conformity with the procedures described in the following literature:
LDAR test: J. Pharm. Soc. Japan, 98, 376(1978)
HAIR test: Acta Endocr. (Kbh), Suppl. 70(1962)
Lower portions of polyethylene tubes with an inside diameter of 5 mm and a height of 45 mm were respectively packed with 50 mg of the above fibers according to this invention and the filtration procedure described hereinbefore was followed to obtain 0.3 ml of filtered urine or serum. As the cellulosic filter paper, Toyo Filter No. 50 (dia. 5.5 cm, wt. 237 mg) was used. The paper was pursed and placed over a funnel and 1.5 ml of urine or serum was passed.
As regards subject fluids, 10 urine specimens, with especially high degrees of interference, from those of nonpregnant women were selected. The five serum specimens from nonpregnant women were also employed. Each specimen was filtered as described hereinbefore and submitted to LDAR and HAIR tests. As controls, unfiltered samples were also tested. The results are presented in Table 1 and 2 appearing later.
The unfiltered urine specimens of nonpregnant women used in these tests showed overtly positive results in 5 out of 10 cases in LDAR, with the remaining 5 cases giving doubtful-positive results, i.e. intermediate between negative and positive reactions. In HAIR, one case was positive and 3 cases were doubtful positive. The influence of components leading to false results is particularly evident in LDAR but their incidence is reduced by filtration. The incidences of false results with various filter materials, when doubtful-positive results were added to positive results, were as follows. Cellulosic filter paper 5/10; absorbent cotton 5/10; wool 3/10; untreated glass fiber 3/10; viscose rayon 5/10; nylon 5/10; polyester 5/10; polypropylene 5/10; polyvinyl chloride 5/10; polyacrylonitrile 3/10; polyurethane 4/10; cellulose acetate 2/10; carboxymethylcellulose 1/10.
When the carboxylic acid-type cation exchange resin fiber or siliconized glass fiber was employed, all cases were found to be negative. In HAIR runs using filtered urine, all cases were found to be negative. The results of LDAR runs on nonpregnant sera, filtered through different filters, are shown in Table 3. Without filtration, the incidence of false results was 2/5 but with filtered sera all specimens were found to be negative, irrespective of the filter materials employed.
As mentioned above, when tests are carried out on unfiltered urine or serum, specimens which ought to be negative tend to give positive reactions, thus leading to misdiagnoses. Moreover, even with cellulosic filter paper, absorbent cotton, untreated glass, viscose rayon, nylon, polyester, polypropylene, polyvinyl chloride, polyacrylonitrile, polyurethane, cellulose acetate or carboxymethylcellulose fibers etc., specimens which ought to be negative sometimes produce positive results, thus leading again to misdiagnoses.
LDAR tests were performed on 10 urine samples from women in early stages of pregnancy which were lean in HCG. The results are shown in Table 4. When the urine samples were not filtered, all cases were found to be positive. However, when specimens were filtered through cellulosic filter paper or absorbent cotton, the reaction was considerably weakened so that pregnant women who ought to be positive were falsely found to be nonpregnant. With viscose rayon and carboxymethylcellulose, the incidence of false results was 2/10. The reaction was invariably weak when wool, untreated glass fiber, nylon, polyester, polypropylene, polyvinyl chloride and polyurethane were employed, the incidence of false results being 1/10 for each. In contrast, all cases were found to be positive with the carboxylic acid-type cation exchange resin and siliconized glass fibers according to this invention as well as with polyacrylonitrile and cellulose acetate.
It is necessary to filter subject fluids in order to remove turbidity and interfering components. However, depending on the kind of filter material, the HCG in the test fluid is adsorbed on the filter to cause a misdiagnosis.
When the carboxylic acid-type cation exchange resin or siliconized glass fiber is employed, substantially no HCG adsorption takes place. Moreover, the filters of this invention effectively remove the components which would interfere with the reactions. Thus, they reduce considerably the incidence of misdiagnosing nonpregnancy as pregnancy.
HCG was added to 3 urine samples from healthy nonpregnant women to give an HCG concentration of one I.U./ml, and each sample was filtered as described hereinbefore. The residual HCG (%) in each filtered urine sample was measured by radioimmunoassay.
As shown in Table 5, cellulosic filter paper, absorbent cotton, wool, untreated glass fiber, viscose rayon, nylon, polyester, polypropylene, polyvinyl chloride, polyurethane and carboxymethylcellulose showed up to 65% adsorption of HCG. Substantially no adsorption of HCG occurred with carboxylic acid-type cation exchange resin fiber, siliconized glass fiber, cellulose acetate or polyacrylonitrile fiber.
Polyethylene tubes, 5.0 mm in inside diameter, were respectively packed with 50 mg of carboxylic acid-type cation exchange resin fiber or siliconized glass fiber of the present invention, absorbent cotton, cellulose acetate fiber, polyacrylonitrile fiber and carboxymethylcellulose fiber and 400 urine samples from nonpregnant women were filtered with the above tubes by the procedure described hereinbefore, to obtain 0.3 ml of filtered urine from each urine sample. Two drops of each filtered urine sample were subjected to the LDAR tests.
As shown in Table 6 appearing later, for the urine samples filtered through absorbent cotton, 10 out of 400 samples showed positive reactions and 35 doubtful-positive reactions; with cellulose acetate, 7 positive and 8 doubtful-positive; with polyacrylonitrile, 7 positive and 13 doubtful-positive. With carboxymethylcellulose, too, 1 showed positive reaction and 2 doubtful-positive reactions. On the contrary, with the carboxylic acid-type cation exchange resin fiber or siliconized glass fiber, all the samples (400 samples) gave negative results. In this manner those components which possibly interfere with the diagnostic reaction can be removed to a very great extent by the method of the present invention.
Urine samples from 200 women definitely diagnosed as pregnant by clinical diagnoses were subjected to the LDAR test after filtration under the same conditions as in Example 1 using the carboxylic acid-type cation exchange resin fiber or siliconized glass fiber of the present invention or absorbent cotton, cellulose acetate fiber, polyacrylonitrile fiber or carboxymethylcellulose fiber.
As shown in Table 7 appearing later, in the case of absorbent cotton, polyacrylonitrile and carboxymethylcellulose, 10, 3 and 3 cases, respectively, were erroneously diagnosed as nonpregnant. When the carboxylic acid-type cation exchange resin fiber was used as the filter material according to the invention, all the samples reacted positively in accord with the results of the definite clinical diagnosis. Also in the case where the siliconized glass fiber was used, all the cases showed positive results except for one case in which the reaction was doubtful-positive.
Serum samples from 50 nonpregnant women and 50 pregnant women were filtered through the carboxylic acid-type cation exchange resin fiber or siliconized glass fiber used as a filter material under the same conditions as in Example 1 and two drops of each filtered serum sample were subjected to the LDAR test. All the serum samples from nonpregnant women reacted negatively, while all the serum samples from pregnant women showed positive reactions.
Urine samples from 50 nonpregnant women and 50 pregnant women were filtered through the carboxylic acid-type cation exchange resin staple fiber of 1 mm in length with 3 denier used as a filter material under the same conditions as in Example 1 and two drops of each filtered urine samples were subjected to the LDAR test. All the urine samples from nonpregnant women reacted negatively, while all the urine sample from pregnant women showed positive reactions.
TABLE 1 ______________________________________ Comparison of different pretreatments of urine samples from nonpregnant women (LDAR) Urine No. Pretreatment 1 2 3 4 5 6 7 8 9 10 ______________________________________ Without filtration + + ± ± + ± ± ± + + Filtration through Cellulosic filter paper - + - ± - - ± - ± + Absorbent cotton - + - ± - - ± - ± + Wool - + - - - - - - ± + Untreated glass fiber - + - - - - - - ± + Viscose rayon - + - ± - - ± - ± + Nylon - + - ± - - ± - ± + Polyester - + - ± - - ± - + + Polypropylene - + - ± - - ± - + + Polyvinyl chloride - ± - ± - - ± - + + Polyacrylonitrile - ± - - - - - - ± + Polyurethane - + - - - - ± - ± + Cellulose acetate - - - - - - - - ± + Carboxymethyl- cellulose - - - - - - - - - + Carboxylic acid-type cation exchange resin fiber - - - - - - - - - - Siliconized glass fiber - - - - - - - - - - ______________________________________ Remarks: + Positive results ± Doubtful-position results - Negative results (The same shall apply hereinafter.)
TABLE 2 ______________________________________ Comparison of different pretreatments of urine samples from nonpregnant women (HAIR) Urine No. Pretreatment 1 2 3 4 5 6 7 8 9 10 ______________________________________ Without filtration - ± - - - - - ± ± + Filtration through Cellulosic filter paper - - - - - - - - - - Absorbent cotton - - - - - - - - - - Wool - - - - - - - - - - Untreated glass fiber - - - - - - - - - - Viscose rayon - - - - - - - - - - Nylon - - - - - - - - - - Polyester - - - - - - - - - - Polypropylene - - - - - - - - - - Polyvinyl chloride - - - - - - - - - - Polyacrylonitrile - - - - - - - - - - Polyurethane - - - - - - - - - - Cellulose acetate - - - - - - - - - - Carboxymethyl- cellulose - - - - - - - - - - Carboxylic acid-type cation exchange resin fiber - - - - - - - - - - Siliconized glass fiber - - - - - - - - - - ______________________________________
TABLE 3 ______________________________________ Comparison of different pretreatments of serum samples from nonpregnant women (LDAR) Serum No. Pretreatment 1 2 3 4 5 ______________________________________ Without filtration - - ± - + Filtration through Cellulosic filter paper - - - - - Absorbent cotton - - - - - Wool - - - - - Untreated glass fiber - - - - - Viscose rayon - - - - - Nylon - - - - - Polyester - - - - - Polypropylene - - - - - Polyvinyl chloride - - - - - Polyacrylonitrile - - - - - Polyurethane - - - - - Cellulose acetate - - - - - Carboxymethylcellulose - - - - - Carboxylic acid-type cation exchange resin fiber - - - - - Siliconized glass fiber - - - - - ______________________________________
TABLE 4 ______________________________________ Comparison of different pretreatments of urine samples from women in early stages of pregnancy Urine No. Pretreatment 1 2 3 4 5 6 7 8 9 10 ______________________________________ Without filtration + + + + + + + + + + Filtration through Cellulosic filter paper + - + + ± - - + ± - Absorbent cotton + - + + ± - - + - - Wool + + + + + + + + ± - Untreated glass fiber + + + + + + + + ± - Viscose rayon + ± + + ± - ± + ± - Nylon + + + + + + + + ± - Polyester + + + + + + + + ± - Polypropylene + + + + + + + + ± - Polyvinyl chloride + + + + + + + + ± - Polyacrylonitrile + + + + + + + + + ± Polyurethane + + + + + + + + ± - Cellulose acetate + + + + + + + + + + Carboxymethyl- cellulose + + + + + - + + ± - Carboxylic acid-type cation exchange resin fiber + + + + + + + + + + Siliconized glass fiber + + + + + + + + + + ______________________________________
TABLE 5 ______________________________________ Residual HCG (%) in filtered urine samples Urine No. Pretreatment 1 2 3 ______________________________________ Filtration through Cellulosic filter paper 47 45 50 Absorbent cotton 41 35 40 Wool 62 65 59 Untreated glass fiber 55 60 60 Viscose rayon 40 40 35 Nylon 92 85 88 Polyester 79 80 80 Polypropylene 85 80 75 Polyvinyl chloride 90 88 88 Polyacrylonitrile 100 95 97 Polyurethane 95 86 90 Cellulose acetate 100 99 98 Carboxymethylcellulose 56 60 65 Carboxylic acid-type cation exchange resin 100 101 100 fiber Siliconized glass fiber 100 96 99 ______________________________________
TABLE 6 ______________________________________ Comparison of different pretreatments of urine samples from 400 nonpregnant women Diagnosis (Number of cases) Doubtful- Pretreatment Positive positive Negative ______________________________________ Filtration through Absorbent cotton 10 35 355 Cellulose acetate 7 8 385 Polyacrylonitrile 7 13 380 Carboxymethyl- cellulose 1 2 397 Carboxylic acid-type cation exchange resin fiber 0 0 400 Siliconized glass fiber 0 0 400 ______________________________________
TABLE 7 ______________________________________ Comparison of different pretreatments of urine samples from 200 pregnant women Diagnosis (Number of cases) Doubtful- Pretreatment Positive positive Negative ______________________________________ Filtration through Absorbent cotton 181 9 10 Cellulose acetate 195 2 3 Polyacrylonitrile 193 4 3 Carboxymethyl- cellulose 189 6 5 Carboxylic acid- type cation exchange resin fiber 200 0 0 Siliconized glass fiber 199 1 0 ______________________________________
Claims (6)
1. A method for pretreating a subject fluid for a pregnancy test by means of an immunologic assay of human chorionic gonadotropin, which comprises removing the interfering components and turbidity from the subject fluid by contacting the subject fluid with a carboxylic acid-type cation exchange resin fiber having a cation exchange capacity of about 5 to 8 meq/g or a siliconized glass fiber prepared by impregnating a glass fiber with a solution of dimethylpolysiloxane and heating the fiber.
2. A method according to claim 1, wherein the subject fluid is woman's urine or serum.
3. A method according to claim 1, wherein the subject fluid is filtered through a layer of the carboxylic acid-type cation exchange resin fiber or the siliconized glass fiber.
4. A method according to claim 3, wherein the resin fiber is in the form of filament or staple fiber with a denier number of about 2 to 15.
5. A method according to claim 3, wherein the layer is of the siliconized glass fiber in the form of filament with a diameter of about 5 to 15 μm.
6. A method according to claim 3, wherein the amount of the fibrous layer is about 20 to 100 mg per 0.3 ml of the subject fluid.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP53-160762 | 1978-12-25 | ||
JP53160762A JPS5933228B2 (en) | 1978-12-25 | 1978-12-25 | Pretreatment method and pretreatment agent for test solution for pregnancy diagnosis reaction |
Publications (1)
Publication Number | Publication Date |
---|---|
US4270923A true US4270923A (en) | 1981-06-02 |
Family
ID=15721906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US06/107,179 Expired - Lifetime US4270923A (en) | 1978-12-25 | 1979-12-26 | Pretreatment agent for subject fluid in pregnancy test |
Country Status (8)
Country | Link |
---|---|
US (1) | US4270923A (en) |
JP (1) | JPS5933228B2 (en) |
CA (1) | CA1136972A (en) |
DE (1) | DE2951672A1 (en) |
FR (1) | FR2445528A1 (en) |
GB (1) | GB2040045B (en) |
HK (1) | HK9586A (en) |
MY (1) | MY8500422A (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4536478A (en) * | 1984-04-05 | 1985-08-20 | Seragan Diagnostics, Inc. | Method for reducing non-specific interferences in agglutination immunoassays |
US4600698A (en) * | 1983-01-31 | 1986-07-15 | Hoechst Aktiengesellschaft | Immunological latex agglutination in presence of certain lactones or lactams |
US5202267A (en) * | 1988-04-04 | 1993-04-13 | Hygeia Sciences, Inc. | Sol capture immunoassay kit and procedure |
US20030022390A1 (en) * | 2002-05-30 | 2003-01-30 | Stephens James Matthew | Method and kit for making interfering substances in urine undetectable |
US6867002B2 (en) * | 1998-10-20 | 2005-03-15 | Matsushita Electric Industrial Co., Ltd. | Sample treating kit and sample treating method using the same for analysis with a biosensor |
US7045098B2 (en) | 2001-02-02 | 2006-05-16 | James Matthew Stephens | Apparatus and method for removing interfering substances from a urine sample using a chemical oxidant |
EP1712917A1 (en) * | 2003-12-24 | 2006-10-18 | DENKA SEIKEN Co., Ltd. | Simple membrane assay method and kit |
EP1867991A1 (en) * | 2005-07-25 | 2007-12-19 | Arkray, Inc. | Immunoassay method and immunoassay kit to be used therein |
US20150174509A1 (en) * | 2013-12-20 | 2015-06-25 | Hollingsworth & Vose Company | Filter media with fine staple fibers |
US20150360156A1 (en) * | 2013-12-20 | 2015-12-17 | Hollingsworth & Vose Company | Filter media and elements with fine staple fibers |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1146852A (en) * | 1979-01-31 | 1983-05-24 | Koichi Kondo | Reagent for latex agglutination |
EP0288311A1 (en) * | 1987-04-24 | 1988-10-26 | Pall Corporation | Method of treating urine |
ES2168402T3 (en) * | 1996-03-18 | 2002-06-16 | Stiftung Fur Diagnostische For | IMMUNOANALYSIS IN PARTICLES WITH A COMPACT MATRIX. |
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CA1054515A (en) * | 1975-12-17 | 1979-05-15 | Morris L. Givner | Ultrafiltration in pregnancy diagnosis |
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- 1978-12-25 JP JP53160762A patent/JPS5933228B2/en not_active Expired
-
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- 1979-12-21 FR FR7931526A patent/FR2445528A1/en active Granted
- 1979-12-21 CA CA000342474A patent/CA1136972A/en not_active Expired
- 1979-12-21 GB GB7944182A patent/GB2040045B/en not_active Expired
- 1979-12-21 DE DE19792951672 patent/DE2951672A1/en active Granted
- 1979-12-26 US US06/107,179 patent/US4270923A/en not_active Expired - Lifetime
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- 1985-12-30 MY MY422/85A patent/MY8500422A/en unknown
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- 1986-02-05 HK HK95/86A patent/HK9586A/en unknown
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US3215500A (en) * | 1961-06-12 | 1965-11-02 | Donald L Bittner | Laboratory mixer-separator |
US3171783A (en) * | 1962-08-15 | 1965-03-02 | Hyland Lab | Diagnostic procedure |
US3594993A (en) * | 1966-11-14 | 1971-07-27 | Dexter Corp | Porous, bonded and impregnated, nonwoven filter sheet structure |
US3873682A (en) * | 1971-02-23 | 1975-03-25 | Mochida Pharm Co Ltd | Filter for urine samples to be used in pregnancy tests and method of using same |
US3901657A (en) * | 1974-04-29 | 1975-08-26 | Sun Scient Inc | Device for testing solutions and body fluids |
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4600698A (en) * | 1983-01-31 | 1986-07-15 | Hoechst Aktiengesellschaft | Immunological latex agglutination in presence of certain lactones or lactams |
US4536478A (en) * | 1984-04-05 | 1985-08-20 | Seragan Diagnostics, Inc. | Method for reducing non-specific interferences in agglutination immunoassays |
US5202267A (en) * | 1988-04-04 | 1993-04-13 | Hygeia Sciences, Inc. | Sol capture immunoassay kit and procedure |
US6867002B2 (en) * | 1998-10-20 | 2005-03-15 | Matsushita Electric Industrial Co., Ltd. | Sample treating kit and sample treating method using the same for analysis with a biosensor |
US7045098B2 (en) | 2001-02-02 | 2006-05-16 | James Matthew Stephens | Apparatus and method for removing interfering substances from a urine sample using a chemical oxidant |
US20030022390A1 (en) * | 2002-05-30 | 2003-01-30 | Stephens James Matthew | Method and kit for making interfering substances in urine undetectable |
US20070202611A1 (en) * | 2003-12-24 | 2007-08-30 | Denka Seiken Co., Ltd. | Simple membrane assay method and kit |
EP1712917A4 (en) * | 2003-12-24 | 2007-08-01 | Denka Seiken Kk | Simple membrane assay method and kit |
EP1712917A1 (en) * | 2003-12-24 | 2006-10-18 | DENKA SEIKEN Co., Ltd. | Simple membrane assay method and kit |
US7579195B2 (en) | 2003-12-24 | 2009-08-25 | Denka Seiken Co., Ltd | Simple membrane assay method and kit |
US20090286226A1 (en) * | 2003-12-24 | 2009-11-19 | Denka Seiken Co., Ltd. | Simple membrane assay method and kit |
EP2270508A1 (en) * | 2003-12-24 | 2011-01-05 | DENKA SEIKEN Co., Ltd. | Membrane assay method and kit |
US8404479B2 (en) | 2003-12-24 | 2013-03-26 | Denka Seiken Co., Ltd | Simple membrane assay method and kit |
EP1867991A1 (en) * | 2005-07-25 | 2007-12-19 | Arkray, Inc. | Immunoassay method and immunoassay kit to be used therein |
EP1867991A4 (en) * | 2005-07-25 | 2008-06-04 | Arkray Inc | Immunoassay method and immunoassay kit to be used therein |
US20150174509A1 (en) * | 2013-12-20 | 2015-06-25 | Hollingsworth & Vose Company | Filter media with fine staple fibers |
US20150360156A1 (en) * | 2013-12-20 | 2015-12-17 | Hollingsworth & Vose Company | Filter media and elements with fine staple fibers |
Also Published As
Publication number | Publication date |
---|---|
FR2445528B1 (en) | 1985-01-11 |
GB2040045B (en) | 1983-05-11 |
DE2951672A1 (en) | 1980-07-03 |
DE2951672C2 (en) | 1987-10-08 |
CA1136972A (en) | 1982-12-07 |
GB2040045A (en) | 1980-08-20 |
MY8500422A (en) | 1985-12-31 |
JPS5587048A (en) | 1980-07-01 |
JPS5933228B2 (en) | 1984-08-14 |
FR2445528A1 (en) | 1980-07-25 |
HK9586A (en) | 1986-02-14 |
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